"Genome-Nilou Lab"[submitter] AND "RANBP2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 155862	NM_022336.4(EDAR):c.*42G>T	EDAR, RANBP2	Single nucleotide variant (3 prime UTR variant)	Hypohidrotic Ectodermal Dysplasia, Dominant +4 more	GBenign
Select item 5858	NM_022336.4(EDAR):c.1109T>C (p.Val370Ala)	EDAR, RANBP2 (V370A)	Single nucleotide variant (missense variant)	Hypohidrotic Ectodermal Dysplasia, Dominant +6 more	GBenign
Select item 155865	NM_022336.4(EDAR):c.1056C>T (p.Cys352=)	EDAR, RANBP2	Single nucleotide variant (synonymous variant)	Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant +6 more	GBenign
Select item 155864	NM_022336.4(EDAR):c.1024+44C>T	EDAR, RANBP2	Single nucleotide variant (intron variant)	Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant +2 more	GBenign
Select item 155870	NM_022336.4(EDAR):c.750C>T (p.Ser250=)	EDAR, RANBP2	Single nucleotide variant (synonymous variant)	Autosomal recessive hypohidrotic ectodermal dysplasia syndrome +6 more	GBenign
Select item 155867	NM_022336.4(EDAR):c.655+30T>C	EDAR, RANBP2	Single nucleotide variant (intron variant)	Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant +2 more	GBenign

ClinVar